• Job Description

  Req#: SHafWko9awCl
  Clinical Research Coordinator
  
  Noho LabsRemote | Full-time
  
  About Noho Labs
  
  Noho Labs is building at the intersection of performance, longevity, and personalized medicine. Through clinician-led education and a safety-first approach, Noho helps patients explore evidence-based therapies, including peptides, with more rigor, better oversight, and higher quality standards than much of the broader market. Noho Labs partners with a physician-led telehealth practice focused on whole-body optimization, longevity, and wellness.
  
  About the Role
  
  Noho Labs is seeking a Clinical Research Coordinator to help launch and operate human clinical research studies focused on peptides, safety, tolerability, and early signals of efficacy in real-world care settings.
  
  This role is ideal for someone who wants meaningful ownership at an early-stage company and is excited by the opportunity to help build the research engine behind a modern longevity and performance platform. The coordinator will work across study startup, patient recruitment, data collection, regulatory coordination, and dissemination of findings. This is not a passive support role. It is a highly hands-on position for someone who is organized, analytical, comfortable with ambiguity, and motivated by the chance to help shape how high-quality clinical evidence is generated in an emerging category.
  
  What You'll Do
  
  Study startup and regulatory coordination
  
  • Support IRB submission processes, including Advarra-related documentation and correspondence
  • Conduct literature reviews to inform protocol development and study materials
  • Draft informed consent forms, recruitment materials, case report forms, and other regulatory documents
  • Help organize investigator, site, and study files to support compliant research operations
  • Build and QA study questionnaires, intake flows, and research data collection tools
  
  
  Study operations and recruitment
  
  • Coordinate patient recruitment, screening, enrollment, and follow-up workflows
  • Help operationalize study launch across Noho's clinical and research infrastructure
  • Track milestones, deadlines, and participant progress across active studies
  • Maintain accurate, organized, high-integrity research records and datasets
  • Partner with internal stakeholders to improve research workflows, dashboards, and reporting
  
  
  Data, reporting, and dissemination
  
  • Clean, organize, and manage study data for interim review and final analysis
  • Prepare preliminary data summaries and internal presentations
  • Support external presentations, abstracts, posters, and manuscript development
  • Work with statistical and clinical partners to help translate findings into credible, decision-useful outputs
  
  What Success Looks Like
  
  • Studies launch on time with strong operational structure and clean documentation
  • Recruitment and follow-up processes run smoothly
  • Research data is accurate, well organized, and usable for analysis
  • Internal teams have visibility into study progress and outcomes
  • Noho builds a stronger evidence base around peptide use, patient safety, and clinical outcomes
  
  
  Who This Role Is For
  
  This role is well suited for a post-baccalaureate candidate, graduate student, or early-career clinical research professional interested in:
  
  • clinical research
  • longevity and performance medicine
  • peptide therapeutics
  • human subjects research
  • digital health or telehealth-enabled care
  • research operations at an early-stage company
  
  
  Preferred Background
  
  • Prior experience in clinical research, human subjects research, or healthcare research coordination
  • Familiarity with IRB processes, informed consent, and research documentation
  • Strong writing skills, especially for study materials, summaries, and presentations
  • Comfort working with data collection tools, spreadsheets, and structured datasets
  • Strong attention to detail and ability to manage multiple workstreams at once
  • Interest in peptides, personalized medicine, chronic illness, recovery, or novel therapeutics
  • Experience with remote research operations, patient-facing coordination, or startup environments is a plus

• About the company

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